Variant report

Variant rs4773909
Chromosome Location chr13:96150717-96150718
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:96145000-96152600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr13:96149000-96152200 Enhancers Cortex derived primary cultured neurospheres brain
3 chr13:96149200-96150800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr13:96149200-96151800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr13:96149600-96150800 Enhancers Fetal Muscle Trunk muscle
6 chr13:96149600-96150800 Enhancers Left Ventricle heart
7 chr13:96149600-96150800 Enhancers Rectal Smooth Muscle rectum
8 chr13:96149600-96152800 Enhancers Primary monocytes fromperipheralblood blood
9 chr13:96149600-96152800 Enhancers Monocytes-CD14+_RO01746 blood
10 chr13:96150000-96151000 Weak transcription Primary neutrophils fromperipheralblood blood
11 chr13:96150200-96150800 Enhancers Colon Smooth Muscle Colon
12 chr13:96150200-96151200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr13:96150600-96150800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr13:96150600-96151800 Weak transcription Primary hematopoietic stem cells short term culture blood
15 chr13:96150600-96157800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr13:96150600-96166800 Weak transcription Pancreas Pancrea
17 chr13:96150600-96167800 Weak transcription Esophagus oesophagus

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